| # | | Name | Source | Ver | Description |
| 1 | | Adverse Event Expectation | hl7.fhir.us.ctcae#current | R4 | A determination if the adverse event is or is not one whose nature and severity have been previously observed, identified in nature, severity, or frequency, and documented in the investigator brochure, investigational plan, protocol, current consent form, scientific publication, or in other relevant and reliable document. |
| 2 | | Adverse Event Resolved Date | hl7.fhir.us.ctcae#current | R4 | The date (and time) when the adverse event ends or returns to baseline (NCI Thesaurus). |
| 3 | | Adverse Event Resolved Date | hl7.fhir.us.pedcan#current | R4 | The date (and time) when the adverse event ends or returns to baseline (NCI Thesaurus). |
| 4 | | AgeAtTimeOfOnset | hl7.fhir.us.icsr-ae-reporting#current | R4 | The age of the patient when the event occurred. |
| 5 | | CTC Adverse Event Grade | hl7.fhir.us.ctcae#current | R4 | The grade associated with the severity of an adverse event, using CTCAE criteria. The code '0' representing no adverse event may be used to provide positive confirmation that the clinician assessed or considered this particular AE, although the absence of an adverse event is generally not reportable. See https://ctep.cancer.gov/protocolDevelopment/electronic_applications/ctc.htm |
| 6 | | CTC Adverse Event Grade | hl7.fhir.us.pedcan#current | R4 | The grade associated with the severity of an adverse event, using CTCAE criteria. The code '0' representing no adverse event may be used to provide positive confirmation that the clinician assessed or considered this particular AE, although the absence of an adverse event is generally not reportable. See https://ctep.cancer.gov/protocolDevelopment/electronic_applications/ctc.htm |
| 7 | | DeathCause | hl7.fhir.us.cdmh#current | R4 | Death Cause. |
| 8 | | EventDuration | hl7.fhir.us.icsr-ae-reporting#current | R4 | The duration of the adverse event. |
| 9 | | EventEndDate | hl7.fhir.us.icsr-ae-reporting#current | R4 | When the event ended. |
| 10 | | EventSeriousness | hl7.fhir.us.icsr-ae-reporting#current | R4 | Additional codes that give more detail around the adverse event seriousness. |
| 11 | | PCORNet Death Cause Code | hl7.fhir.us.cdmh#current | R4 | Death Cause Code. |
| 12 | | PCORNet Death Cause Confidence | hl7.fhir.us.cdmh#current | R4 | Death Cause Confidence. |
| 13 | | PCORNet Death Cause Source | hl7.fhir.us.cdmh#current | R4 | Death Cause Source. |
| 14 | | PCORNet Death Cause Type | hl7.fhir.us.cdmh#current | R4 | Death Cause Type. |
| 15 | | PCORNet Death Match Confidence | hl7.fhir.us.cdmh#current | R4 | Death Match Confidence. |
| 16 | | PCORNet Death Source Code | hl7.fhir.us.cdmh#current | R4 | Death Source Type. |
| 17 | | Radiotherapy Adverse Event Grade | hl7.fhir.us.codex-radiation-therapy#current | R4 | The grade associated with the severity of an adverse event, using CTCAE criteria. The code '0' representing no adverse event may be used to provide positive confirmation that the clinician assessed or considered this particular AE, although the absence of an adverse event is generally not reportable. See https://ctep.cancer.gov/protocolDevelopment/electronic_applications/ctc.htm |